Summary
Prediction of the impact of climate change requires the response of carbon (C) flow in plant–soil systems to increased CO2 to be understood.
A mechanism by which grassland C sequestration might be altered was investigated by pulse‐labelling Lolium perenne swards, which had been subject to CO2 enrichment and two levels of nitrogen (N) fertilization for 10 yr, with 14CO2.
Over a 6‐d period 40–80% of the 14C pulse was exported from mature leaves, 1–2% remained in roots, 2–7% was lost as below‐ground respiration, 0.1% was recovered in soil solution, and 0.2–1.5% in soil. Swards under elevated CO2 with the lower N supply fixed more 14C than swards grown in ambient CO2, exported more fixed 14C below ground and respired less than their high‐N counterparts. Sward cutting reduced root 14C, but plants in elevated CO2 still retained 80% more 14C below ground than those in ambient CO2.
The potential for below‐ground C sequestration in grasslands is enhanced under elevated CO2, but any increase is likely to be small and dependent upon grassland management.
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Neolithic man probably used fertilizers, but the first fertilizer produced by chemical processes was ordinary superphosphate, made early in the 19th century by treating bones with sulfuric acid. Coprolites and phosphate rock soon replaced bones as the P source. The K fertilizer industry started in Germany in 1861. In North America the K industry started during World War I and expanded with development of the New Mexico deposits in 1931 and the Saskatchewan deposits in 1958. Modern K fertilizers are more the product of physical than of chemical processes. The first synthetic N fertilizer was calcium nitrate, made in 1903 from nitric acid produced by the electric arc process. The availability of synthetic ammonia after 1913 led to many new N fertilizers, but physical quality was poor. In 1933 TVA was formed with a national responsibility to increase the efficiency of fertilizer manufacture and use. More than 75% of the fertilizer produced in the United States is made with processes developed by TVA.Major fertilizers and fertilizer intermediates introduced by TVA include ammonium nitrate, high‐analysis phosphates, diammonium phosphate, nitric phosphates, ammonium polyphosphate, urea ammonium phosphates, 11‐16‐0 and other liquid base solutions, superphosphoric acid, wet‐process superphosphoric acid, suspensions, granular urea, and S‐coated urea. These have had major impact upon the production of mixed fertilizers, bulk blending, and the fluid fertilizer industry. Future fertilizers not only must be technologically feasible, economical, and agronomically suitable—as have been past fertilizers—but also must meet various air and water pollution standards during production and have reduced total energy requirements.
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